Merck KGaA
Senior Specialist Medical Writer
Job Description
About the RoleAs a Senior Specialist Medical writer , you will support the Global Medical Writing Team to deliver its portfolio effectively and efficiently. Independently author clinical and regulatory documents in collaboration with a particular focus on Investigator Brochures (IBs) and INDs/IMPDs.Thoroughly analyze and critically interpret data to determine the best approach to composing each document.Participate in meetings related to key MW, QC, and compliance activitiesCollaborate cross functionally for continuous improvement of for medical writing Who you are:Graduate or post graduate degree in BPharm/MPharm, PHD, BDS (Dental), BSC/MSC or equivalent job experience with comprehensive Medical Writing knowledge of theories, principles and concepts, MD/PhD or advanced science degree.Regulatory medical writing experience (4 to 9 years)Excellent written and spoken English (including medical terminology) and familiarity with AMA style guide.Knowledge of Clinical and Regulatory documents We are an equal opportunity employer that values workforce diversity. We want everyone to be able to bring their best self to work every day which is why equality and inclusion is at the forefront of all our activities. We are dedicated to a policy of non-discrimination in employment on any basis including race, caste, creed, colour, religion, sex, age, disability, marital status, sexual orientation, and gender identity.
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